000 01427nam a2200325Ia 4500
001 289244
003 OCoLC
005 20160527201943.0
008 080721s2008 ne a b 001 0 eng d
015 _aGBA8A4911
_2bnb
020 _a9780123745279
020 _a0123745276
035 _a(OCoLC)234450069
040 _aBTCTA
_cBTCTA
_dBAKER
_dYDXCP
_dTHM
_dMTG
_dUKM
049 _aPUXA
050 4 _aQH431.A1
_bA3 V.63
082 0 4 _a571.64
_222
082 0 4 _a616.07
_222
092 0 _a575.1
_bA244
245 0 0 _aIon channel diseases
_cedited by Guy Rouleau, Claudia Gaspar.
260 _aAmsterdam
_aBoston
_bAcademic Press
_cc2008.
300 _ax, 157 p.
_bill.
_c24 cm.
490 0 _aAdvances in genetics
_vv. 63
_2Local
_949476
504 _aIncludes bibliographical references and index.
505 0 0 _tPeriodic paralysis
_rBertrand Fontaine --
_tMyotonia congenita
_rChristoph Lossin and Alfred L. George, Jr. --
_tFamilial hemiplegic migraine
_rCurtis F. Barrett ... [et al.] --
_tGenetics and molecular pathophysiology of Na [v below line] 1.7-related pain syndromes
_rSulayman D. Dib-Hajj, Yong Yang, and Stephen G. Waxman --
_tChannelopathies of transepithelial transport and vesicular function
_rChristian A. Hübner and Thomas J. Jentsch.
650 0 _aIon channels.
_2Local
_9115964
650 0 _aMembrane disorders.
_2Local
_9134958
700 1 _aRouleau, Guy.
_2Local
_9162560
700 1 _aGaspar, Claudia.
_2Local
_9101382
999 _c209333
_d209333